Evidence map›Paper›PMID 36628228›Full record

ArticleAmerican journal of translational research2022

Angiotensinogen, a promising gene signature for rectum and stomach adenocarcinoma patients.

Wei Hu, Mostafa A Abdel-Maksoud, Syed Yousaf Khalid, Abdul Malik, Musaed Alkholief, Ayman Mubarak, Mohammed Aufy

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Wei HuThe Fourth Clinical Medical College of Yangzhou University, Nantong Rich Hospital Nantong 226010, Jiangsu, China.
Mostafa A Abdel-MaksoudDepartment of Botany and Microbiology, College of Science, King Saud University P. O. 2455, Riyadh 11451, Saudi Arabia.
Syed Yousaf KhalidDepartment of General Surgery, Letterkenny University Hospital Ireland.
Abdul MalikDepartment of Pharmaceutics, College of Pharmacy, King Saud University Riyadh, Saudi Arabia.
Musaed AlkholiefDepartment of Pharmaceutics, College of Pharmacy, King Saud University Riyadh, Saudi Arabia.
Ayman MubarakDepartment of Botany and Microbiology, College of Science, King Saud University P. O. 2455, Riyadh 11451, Saudi Arabia.
Mohammed AufyDepartment of Pharmaceutical Sciences, Division of Pharmacology and Toxicology, University of Vienna Vienna, Austria.
King Saud University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAngiotensinogen (AGT), as a component of the renin-angiotensin system (RAS), is one of the major risk factors for cancer development. To date, there has not been a systematic pan-cancer analysis of AGT.

methodsThis pan-cancer study comprehensively investigated AGT in 24 different cancers based on the UALCAN, KM plotter, GENT2, HPA, MEXPRESS, cBioportal, STRING, TIMER, and CTD databases.

resultsThe results showed that AGT was highly expressed in most tumors, and AGT overexpression may be related to the worst survival of Rectum adenocarcinoma (READ) and Stomach Adenocarcinoma (STAD) patients only. Furthermore, pathway analysis indicated that AGT-associated genes are involved in six critical pathways. Moreover, the higher expression of AGT was found to be detrimental to the promoter methylation level (P<0.05), immune cells infiltration (P<0.05), and genetic alterations. We have also predicted various chemotherapeutic drugs contributing to the expression regulation of AGT.

conclusionOur results together support that AGT is a possible biomarker for READ and STAD.

Indexed as

AGTbiomarkerdiagnosticprognosticREADSTAD

Identifiers

PMID36628228
PMCPMC9827296
OpenAlexW4315619302

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.